“Those who live with a rare disease often feel alone. This is why we believe in the value of unity: just like a team working toward a common goal, families together can find strength and mutual support. Our aim is to build a more inclusive and attentive community.” These are the words of Francesca Cappello, President of the association Diversamente Genitori, describing the spirit of a long-standing collaboration that sees Como 1907 and the local community working together for a cause that touches everyone.
From February 28 to March 8, 2026, the province of Como comes together for a new edition of Un Dolce Raro, the solidarity initiative promoted by Diversamente Genitori on the occasion of International Rare Disease Day. The initiative involves local pastry chefs and bakers who have created “special” sweets for this week: for each purchase, the businesses selling the treats commit to donating a portion of the proceeds to Diversamente Genitori.
This collaboration helps fund Il Sogno di Zeno, a project that provides training in Augmentative and Alternative Communication (AAC) for educators and teachers in local schools. AAC, a symbol-based language used by people with complex verbal communication difficulties, is an essential tool for social integration. Thanks to the funds raised, schools in the area can join the project free of charge and receive support from experts to break down isolation barriers, reduce stress and frustration and enable students to participate actively in lessons.
Como 1907’s support was particularly tangible during the home match against Lecce on February 28, coinciding with Rare Disease Day. Fondazione Como ETS purchased and distributed a supply of solidarity muffins in the hospitality areas during halftime, while the “Dolce Raro” was sold at the stadium bars, giving all fans the opportunity to contribute and come together for a cause that concerns the entire community.
Diversamente Genitori was founded to guide and support families receiving a diagnosis of disability or rare disease, a moment that often marks a turning point in the life of a family. Rare Disease Day is a key occasion to shine a spotlight on conditions often referred to as “orphaned,” due to limited awareness, resources, and treatments. In this context, Un Dolce Raro transforms remembrance into active support.
Over the years, the response from the local community has grown significantly. “The wave of solidarity shows us that we are addressing a real need,” emphasizes Francesca Cappello. “Como 1907, as a symbol of the territory, has the ability to unite diverse people under a single banner. Bringing the topic of rare diseases into the stadium allows us to reach thousands of fans and fight indifference, reminding every family that they are not alone.”
A message that underlines how, when a community moves together, inclusion becomes a shared responsibility.